• Skip to primary navigation
  • Skip to main content
  • Skip to footer

LKT Labs

Biochemicals for Life Science Research

  • Products
    • New Products
    • Cancer Biology
    • Cardiovascular
    • Endocrine Signaling and Immunology
    • Metabolic and GI Pathology
    • Microbiology
    • Natural Products
    • Neuroscience
    • Peptides
    • Pharmaceutical Impurities and Derivatives
    • Stem Cell Modulators
  • Services
    • Custom Synthesis
    • Natural Product Isolation
    • Analytical Services
  • Int’l Distributors
  • Support
    • About LKT Labs
    • General Inquiry
    • Bulk Quote Request
    • Document Request
    • Technical Support
    • Catalog Request
    • Product Flyers
  • Contact Us
  • Cart
  • Login / Register
4-O-Methylhonokiol

4-O-Methylhonokiol

Product ID M184770
Cas No. 68592-15-4
Purity ≥98%
Product Unit SizeCostQuantityStock
5 mg $147.00 In stock
10 mg $267.00 In stock
25 mg $601.00 In stock
100 mg $1,878.00 In stock
Bulk Quote

Quicklinks

  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Custom Order

Description

4-O-Methylhonokiol is a major bioactive constituent of Magnolia officinalis stem bark. In a study with C57BK/6J mice, 4-O-methylhonokiol prevented high-fat-diet induced obesity and insulin resistance, in addition to restoring impaired cardiac insulin signaling. In another study using female RjOrl mice, 4-O-methylhonokiol was shown to act as a central nervous system penetrating substrate-specific inhibitor of COX-2 and as a CB2 receptor agonist. Furthermore, in high-risk HPV-16 genotype SiHa cells, treatment with 4-O-methylhonokiol suppressed the PI3K/Akt signaling pathway thereby reducing the survival of the cells. 4-O-methylhonokiol has also shown several other biological activities including anti-inflammatory, antithrombotic, anti-anxiety, antimicrobial, and anti-HIV activities.

Product Info

Cas No.

68592-15-4

Purity

≥98%

Formula

C19H20O2

Formula Wt.

280.37

Chemical Name

2-(4-Methoxy-3-prop-2-enylphenyl)-4-prop-2-enylphenol

IUPAC Name

2-(4-Methoxy-3-prop-2-enylphenyl)-4-prop-2-enylphenol

Synonym

3,5′-Diallyl-2′-hydroxy-4-methoxybiphenyl, 4-O-methyl honokiol.

Appearance

Clear/yellow oil

Shipping and Storage

Store Temp

4°C

Ship Temp

Ambient

Downloads

MSDS

M184770 MSDS PDF

Info Sheet

M184770 Info Sheet PDF

References

Kim SC, Kang JI, Hyun JW, et al. 4-O-Methylhonokiol protects HaCaT cells from TFG-beta1-induced cell cycle arrest by regulating of canonical and non-canonical pathways of TGF-beta signaling. Biomol Ther (Seoul). 2017 Feb 13. [epub ahead of print] PMID: 28190316.

Zhang Z, Chen J, Zhou S, et al. Magnolia bioactive constituent 4-O-methylhonokiol prevents the impairment of cardiac insulin signaling and the cardiac pathogenesis in high-fat diet-induced obese mice. Int J Biol Sci. 2015 Jun 5;11(8):879-891. PMID: 26157343.

Chicca A, Gachet MS, Petrucci V, et al. 4’-O-Methylhonokiol increases levels of 2-arachidonoyl glycerol in mouse brain via selective inhibition of its COX-2-mediated oxygenation. J Neuroinflammation. 2015 May 13;12:89. PMID: 25962384.

Han JY, Ahn SY, Yoo JH, et al. Alleviation of kainic acid-induced brain barrier dysfunction by 4-O-methylhonokiol in in vitro and in vivo models. Biomed Res Int. 2015;2015:893163. PMID: 25688368.

Hyun S, Kim MS, Song YS, et al. Peroxisome proliferator-activated receptor-gamma agonist 4-O-methylhonokiol induces apoptosis by triggering the intrinsic apoptosis pathway and inhibiting the PI3K/Akt survival pathway in SiHa human cervical cancer cells. J Microbiol Biotechnol. 2015 Mar;25(3):334-342. PMID: 25563418.

Custom Order

  • Size of single unit expressed as number (e.g. '500' in the case of 500 mg)
  • Total quantity of unit size desired (e.g. '10' in the case of 10 x 500 mg). If only one unit is desired, you may leave this blank.
  • This field is for validation purposes and should be left unchanged.

Related Products

  • K0652

    Kb NB 142-70

    PKD inhibitor.

    ≥98%
  • C2948

    Chloroadenosine

    Nucleoside (adenosine) analog; DNA chain termin...

    ≥98%
  • M3309

    Miconazole

    Imidazole; 14-α demethylase inhibitor, potenti...

    ≥98%
  • F3354

    Finasteride

    Steroid 5-α-reductase inhibitor.

    ≥98%
  • C7992

    CTX-0294885

    Bisaniline pyrimidine; pan-kinase inhibitor.

    ≥98%
  • C5654

    Concanavalin A

    Lectin found in Canavelia, plant mitogen that b...

  • C1624

    Cefuroxime Sodium

    β-lactam; penicillin binding protein inhibitor...

    ≥98%
  • P1853

    Penicillin V Potassium

    Hydrophobic β-lactam; penicillin binding prote...

    ≥98%
  • M5610

    Moclobemide

    MAO-A inhibitor.

    ≥98%
  • T6830

    Triadimefon

    Neurotoxin, mutagen.

    ≥98%
  • G3357

    Ginkgolide C

    Diterpene lactone found in Ginkgo; GABA-A, α-1...

    ≥98%
  • N8660

    NVP-AUY922

    Isoxazole derivative; HSP90 inhibitor.

    ≥98%
  • T3034

    Thienylethyl Isothiocyanate

    Thienylbutyl ITC analog.

    ≥98%
  • G0146

    Galanin, human

    Endogenous neuropeptide, involved in nociceptio...

    ≥98%
  • T8153

    Tunicamycin

    Nucleoside antibiotic mixture; GlcNAc phosphotr...

    ≥98%
  • V3476

    Vitamin D2

    Vitamin D prodrug produced by fungi and alfalfa...

    ≥91%
  • A1217

    Adefovir

    Acyclic nucleotide (adenosine) analog; viral DN...

    ≥98%
  • R580665

    Roquefortine C

    Mycotoxin produced by various fungi including t...

    ≥98%
  • S1810

    Secnidazole

    Nitroimidazole, binds DNA; nucleic acid synthes...

    ≥98%
  • A5283

    [Sar1]-Angiotensin II

    Peptide, derivative of AT II, involved in vasoc...

    ≥95%

Footer

  • Contact Us
  • About Us
  • Site Map
  • Terms and Conditions
LKT Laboratories, Inc.
545 Phalen Blvd.
St. Paul MN, 55130

Ph: (888)-558-5227
Fax: (888)-558-7329

©2026 LKT Laboratories, All Rights Reserved - Products for research use only